SELENOM (selenoprotein M) - Rat Genome Database

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Gene: SELENOM (selenoprotein M) Homo sapiens
Analyze
Symbol: SELENOM
Name: selenoprotein M
RGD ID: 1603181
HGNC Page HGNC:30397
Description: Predicted to enable oxidoreductase activity. Predicted to act upstream of or within several processes, including adipose tissue development; corticosterone secretion; and response to selenium ion. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and perinuclear region of cytoplasm. Predicted to be active in endoplasmic reticulum lumen.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MGC40146; selenoprotein SelM; SELM; SEPM
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382231,104,777 - 31,107,568 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2231,104,772 - 31,120,069 (-)EnsemblGRCh38hg38GRCh38
GRCh372231,500,763 - 31,503,554 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362229,830,763 - 29,833,551 (-)NCBINCBI36Build 36hg18NCBI36
Celera2215,300,895 - 15,303,683 (-)NCBICelera
Cytogenetic Map22q12.2NCBI
HuRef2214,462,570 - 14,465,358 (-)NCBIHuRef
CHM1_12231,460,600 - 31,463,388 (-)NCBICHM1_1
T2T-CHM13v2.02231,568,276 - 31,571,067 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11839807   PMID:12477932   PMID:15489334   PMID:18029348   PMID:21873635   PMID:24284396   PMID:24332979   PMID:25416956   PMID:25578973   PMID:26186194   PMID:27645994   PMID:28514442  
PMID:31274247   PMID:31470122   PMID:31536960   PMID:31768845   PMID:32296183   PMID:33961781   PMID:35696571   PMID:38113892  


Genomics

Comparative Map Data
SELENOM
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382231,104,777 - 31,107,568 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2231,104,772 - 31,120,069 (-)EnsemblGRCh38hg38GRCh38
GRCh372231,500,763 - 31,503,554 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362229,830,763 - 29,833,551 (-)NCBINCBI36Build 36hg18NCBI36
Celera2215,300,895 - 15,303,683 (-)NCBICelera
Cytogenetic Map22q12.2NCBI
HuRef2214,462,570 - 14,465,358 (-)NCBIHuRef
CHM1_12231,460,600 - 31,463,388 (-)NCBICHM1_1
T2T-CHM13v2.02231,568,276 - 31,571,067 (-)NCBIT2T-CHM13v2.0
Selenom
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39113,464,684 - 3,467,351 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl113,464,684 - 3,467,351 (+)EnsemblGRCm39 Ensembl
GRCm38113,514,684 - 3,517,351 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl113,514,684 - 3,517,351 (+)EnsemblGRCm38mm10GRCm38
MGSCv37113,414,705 - 3,417,354 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36113,414,889 - 3,417,353 (+)NCBIMGSCv36mm8
Celera114,005,593 - 4,008,243 (+)NCBICelera
Cytogenetic Map11A1NCBI
cM Map112.47NCBI
Selenom
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81482,619,453 - 82,622,056 (+)NCBIGRCr8
mRatBN7.21478,395,826 - 78,398,429 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1478,395,826 - 78,398,429 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1482,837,015 - 82,839,618 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01484,077,121 - 84,079,724 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01480,522,884 - 80,525,488 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01483,752,393 - 83,754,975 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1483,752,393 - 83,754,973 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01484,440,340 - 84,442,922 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41484,157,831 - 84,160,413 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1477,308,292 - 77,310,874 (+)NCBICelera
Cytogenetic Map14q21NCBI
Selenom
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554555,294,503 - 5,296,748 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554555,294,317 - 5,303,621 (-)NCBIChiLan1.0ChiLan1.0
SELENOM
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22341,060,364 - 41,063,439 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12243,758,865 - 43,761,940 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02212,128,513 - 12,131,653 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12229,966,405 - 29,981,171 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2229,966,602 - 29,969,137 (-)Ensemblpanpan1.1panPan2
SELENOM
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12624,108,342 - 24,111,005 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2624,108,344 - 24,111,005 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2623,978,426 - 23,981,088 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02624,491,085 - 24,493,748 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2624,491,279 - 24,493,748 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12624,194,481 - 24,197,142 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02624,456,479 - 24,459,142 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02624,517,767 - 24,520,429 (-)NCBIUU_Cfam_GSD_1.0
Selenom
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118117,028,301 - 117,030,935 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936755286,030 - 288,246 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936755285,836 - 288,501 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SELENOM
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1447,902,864 - 47,905,440 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11447,902,862 - 47,905,350 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21451,014,556 - 51,017,049 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SELENOM
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11913,996,307 - 13,999,083 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666045112,120,543 - 112,123,317 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Selenom
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247477,582,446 - 7,584,673 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247477,582,259 - 7,584,903 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SELENOM
2 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3 copy number gain See cases [RCV000050768] Chr22:18178957..31821193 [GRCh38]
Chr22:18661724..32217179 [GRCh37]
Chr22:17041724..30547179 [NCBI36]
Chr22:22q11.21-12.3		 pathogenic
GRCh38/hg38 22q12.1-12.3(chr22:26979579-33992220)x3 copy number gain See cases [RCV000050553] Chr22:26979579..33992220 [GRCh38]
Chr22:27375542..34388209 [GRCh37]
Chr22:25705542..32718209 [NCBI36]
Chr22:22q12.1-12.3		 pathogenic
GRCh38/hg38 22q12.1-12.2(chr22:28278805-31742328)x1 copy number loss See cases [RCV000052870] Chr22:28278805..31742328 [GRCh38]
Chr22:28674793..32138314 [GRCh37]
Chr22:27004793..30468314 [NCBI36]
Chr22:22q12.1-12.2		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3 copy number gain See cases [RCV000138172] Chr22:23279231..36247369 [GRCh38]
Chr22:23621418..36643415 [GRCh37]
Chr22:21951418..34973361 [NCBI36]
Chr22:22q11.23-12.3		 pathogenic
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 copy number gain See cases [RCV000137926] Chr22:20907226..37187347 [GRCh38]
Chr22:21261514..37583387 [GRCh37]
Chr22:19591514..35913333 [NCBI36]
Chr22:22q11.21-12.3		 pathogenic
GRCh38/hg38 22q12.1-12.2(chr22:26451042-31451926)x1 copy number loss See cases [RCV000143415] Chr22:26451042..31451926 [GRCh38]
Chr22:26847008..31847912 [GRCh37]
Chr22:25177008..30177912 [NCBI36]
Chr22:22q12.1-12.2		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.1-12.3(chr22:28349854-33013062)x3 copy number gain See cases [RCV000510523] Chr22:28349854..33013062 [GRCh37]
Chr22:22q12.1-12.3		 likely pathogenic
GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3 copy number gain See cases [RCV000511098] Chr22:23637907..36614412 [GRCh37]
Chr22:22q11.23-12.3		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.22-12.3(chr22:22460754-35198232)x3 copy number gain not provided [RCV000684530] Chr22:22460754..35198232 [GRCh37]
Chr22:22q11.22-12.3		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
inv(22)(q12.2q12.2) inversion Anaplastic ependymoma [RCV000785873] Chr22:29684716..31740655 [GRCh37]
Chr22:22q12.2		 likely pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_080430.4(SELENOM):c.152A>G (p.Asn51Ser) single nucleotide variant Inborn genetic diseases [RCV003250883] Chr22:31105943 [GRCh38]
Chr22:31501929 [GRCh37]
Chr22:22q12.2		 uncertain significance
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NC_000022.10:g.(?_29083885)_(34046674_?)dup duplication not provided [RCV001979643] Chr22:29083885..34046674 [GRCh37]
Chr22:22q12.1-12.3		 uncertain significance
NM_080430.4(SELENOM):c.86C>T (p.Pro29Leu) single nucleotide variant Inborn genetic diseases [RCV003203771] Chr22:31107420 [GRCh38]
Chr22:31503406 [GRCh37]
Chr22:22q12.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3036
Count of miRNA genes:756
Interacting mature miRNAs:897
Transcripts:ENST00000400299, ENST00000402395, ENST00000460642, ENST00000465447, ENST00000465536, ENST00000469262, ENST00000490967, ENST00000491958, ENST00000495533
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-57277  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,500,916 - 31,501,080UniSTSGRCh37
Build 362229,830,916 - 29,831,080RGDNCBI36
Celera2215,301,048 - 15,301,212RGD
Cytogenetic Map22q12.2UniSTS
HuRef2214,462,723 - 14,462,887UniSTS
TNG Radiation Hybrid Map226285.0UniSTS
STS-W72233  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372231,500,344 - 31,500,560UniSTSGRCh37
Build 362229,830,344 - 29,830,560RGDNCBI36
Celera2215,300,476 - 15,300,692RGD
Cytogenetic Map22q12.2UniSTS
HuRef2214,462,151 - 14,462,367UniSTS
GeneMap99-GB4 RH Map2285.97UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 19 136 102 17 9 102
Medium 2309 2163 1440 344 644 183 4071 2093 3648 331 1361 1480 169 1 1204 2651 3 2
Low 90 689 283 277 1206 279 165 81 82 84 78 107 5 35 3
Below cutoff 20 3 3 3 92 3 19 6 4 4 11 25

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000400299   ⟹   ENSP00000383155
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,104,777 - 31,107,568 (-)Ensembl
RefSeq Acc Id: ENST00000402395   ⟹   ENSP00000384564
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,104,772 - 31,120,069 (-)Ensembl
RefSeq Acc Id: ENST00000460642
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,105,025 - 31,107,541 (-)Ensembl
RefSeq Acc Id: ENST00000465447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,105,439 - 31,107,556 (-)Ensembl
RefSeq Acc Id: ENST00000465536
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,104,926 - 31,107,528 (-)Ensembl
RefSeq Acc Id: ENST00000469262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,105,114 - 31,107,466 (-)Ensembl
RefSeq Acc Id: ENST00000490967
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,104,777 - 31,107,533 (-)Ensembl
RefSeq Acc Id: ENST00000491958
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,105,001 - 31,107,553 (-)Ensembl
RefSeq Acc Id: ENST00000495533
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,105,013 - 31,105,764 (-)Ensembl
RefSeq Acc Id: ENST00000611680   ⟹   ENSP00000480176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2231,104,779 - 31,107,568 (-)Ensembl
RefSeq Acc Id: NM_080430   ⟹   NP_536355
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382231,104,777 - 31,107,568 (-)NCBI
GRCh372231,500,763 - 31,503,551 (-)RGD
Build 362229,830,763 - 29,833,551 (-)NCBI Archive
Celera2215,300,895 - 15,303,683 (-)RGD
HuRef2214,462,570 - 14,465,358 (-)RGD
CHM1_12231,460,600 - 31,463,388 (-)NCBI
T2T-CHM13v2.02231,568,276 - 31,571,067 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_536355   ⟸   NM_080430
- Peptide Label: precursor
- UniProtKB: A8MPZ2 (UniProtKB/Swiss-Prot),   Q8WWX9 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000383155   ⟸   ENST00000400299
RefSeq Acc Id: ENSP00000480176   ⟸   ENST00000611680
RefSeq Acc Id: ENSP00000384564   ⟸   ENST00000402395

Promoters
RGD ID:6800248
Promoter ID:HG_KWN:42379
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ENST00000361918,   ENST00000400299,   OTTHUMT00000321790,   OTTHUMT00000321791,   OTTHUMT00000321792,   OTTHUMT00000321793,   OTTHUMT00000321794,   OTTHUMT00000321795,   OTTHUMT00000321796,   UC010GWF.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362229,833,296 - 29,833,796 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30397 AgrOrtholog
COSMIC SELENOM COSMIC
Ensembl Genes ENSG00000198832 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000400299 ENTREZGENE
  ENST00000400299.6 UniProtKB/Swiss-Prot
  ENST00000402395.5 UniProtKB/Swiss-Prot
Gene3D-CATH 3.40.30.50 UniProtKB/Swiss-Prot
GTEx ENSG00000198832 GTEx
HGNC ID HGNC:30397 ENTREZGENE
Human Proteome Map SELENOM Human Proteome Map
InterPro Sep15/SelM_sf UniProtKB/Swiss-Prot
  Sep15_SelM UniProtKB/Swiss-Prot
  Sep15_SelM_dom UniProtKB/Swiss-Prot
  Thioredoxin-like_sf UniProtKB/Swiss-Prot
KEGG Report hsa:140606 UniProtKB/Swiss-Prot
NCBI Gene 140606 ENTREZGENE
OMIM 610918 OMIM
PANTHER PTHR13077 UniProtKB/Swiss-Prot
  SELENOPROTEIN M UniProtKB/Swiss-Prot
Pfam Sep15_SelM UniProtKB/Swiss-Prot
PharmGKB PA166181631 PharmGKB
Superfamily-SCOP SSF52833 UniProtKB/Swiss-Prot
UniProt A8MPZ2 ENTREZGENE
  Q8WWX9 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A8MPZ2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-09-27 SELENOM  selenoprotein M  SELM  selenoprotein M  Symbol and/or name change 5135510 APPROVED